Chloroform → HCID 14346304, compound
Reaction equation
C(Cl)(Cl)Cl.[CH3:5][CH2:6]/[C:7](/[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)=[C:8](/[C:16]1[CH:21]=[CH:20][C:19]([O:22][CH2:23][CH2:24][N:25]([CH3:27])[CH3:26])=[CH:18][CH:17]=1)\[C:9]1[CH:14]=[CH:13][C:12]([OH:15])=[CH:11][CH:10]=1>CC(C)=O>[CH3:5][CH2:6]/[C:7](/[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)=[C:8](/[C:16]1[CH:21]=[CH:20][C:19]([O:22][CH2:23][CH2:24][N:25]([CH3:27])[CH3:26])=[CH:18][CH:17]=1)\[C:9]1[CH:10]=[CH:11][C:12]([OH:15])=[CH:13][CH:14]=1.[CH3:11][C:12]([CH3:13])=[O:15]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
0.1 mol of the chloroform or perchloroethylene complex of Z-4-hydroxytamoxifen from Examples (1c1) and (1c2) are recrystallized from 300 ml of acetone and suction filtered at 10° C.
Workup
- filtrationfiltered at 10° C.
Sources & evidence
- ORD record
- ord-4099fa1a601d42f5ac75158296d6e2d3
- Source dataset
- uspto-grants-1990_11
- Patent number
- US04973755
Reaction notes
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